[Neonatal macrocephaly caused by multiple cerebral arteriovenous fistula treated with embolization techniques]

[Telematic attention in a neuropediatrics consultation during the COVID-19 alarm state. Cross-sectional study and satisfaction survey].

Journal of healthcare quality research·2022

Neurological manifestations of neurofibromatosis type 1: our experience.

Neurologia·2022

A novel mutation in the ZNF462 gene c.3306dup; p.(Gln1103Thrfs*10) is associated to Weiss-Kruszka syndrome. A case report.

Acta clinica Belgica·2020

Neurological manifestations of neurofibromatosis type 1: our experience.

Neurologia·2019

Functional progression of patients with neurological diseases in a tertiary paediatric intensive care unit: Our experience.

Neurologia·2017

Face recognition impairment in small for gestational age and preterm children.

Research in developmental disabilities·2017

[Langerhans' cell histiocytosis: various manifestations with the same histopathologic base].

Anales espanoles de pediatria·2002

[External ventricular assist devices as circulatory support in patients with dilated cardiomyopathy].

Anales espanoles de pediatria·2002

[Comparison of the epidemiological characteristics of neural tube defects classified according to failure of the different points of closure].

Anales espanoles de pediatria·2002

[Cutaneous colonization by Malassezia spp. in neonates].

Anales espanoles de pediatria·2002

[Balloon valvoplasty for critical aortic valve stenosis in neonates].

Anales espanoles de pediatria·2002

[Childhood headache. A diagnostic approach].

Anales espanoles de pediatria·2002

Early sodium channel blocker initiation is associated with better outcomes in KCNQ2 disorders.

Brain : a journal of neurology·2026

Palatal Perforation as a Rare Presentation of Severe Congenital Neutropenia Due to an ELANE Mutation.

Cureus·2026

Median Nerve Entrapment After Intramedullary Nailing of a Pediatric Both-Bone Forearm Fracture: A Rare Case Report.

Case reports in orthopedics·2026

Relapse of Steroid-Dependent Nephrotic Syndrome Despite Long-Term Ciclosporin Therapy in an 11-Year-Old Child: A Case Report and Review on the Management of Nephrotic Syndrome in Children.

Case reports in nephrology·2026

Embryological Basis and Genetic Considerations of Right Lumbar Undescended Caecum with Paracaecal Appendix and Aberrant Vascular Supply.

Acta medica Lituanica·2026

Inhibition Mechanism of Pancreatic KATP Channels by Centipede Toxin.

Research (Washington, D.C.)·2026

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[Neonatal macrocephaly caused by multiple cerebral arteriovenous fistula treated with embolization techniques]

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[Telematic attention in a neuropediatrics consultation during the COVID-19 alarm state. Cross-sectional study and satisfaction survey].

Neurological manifestations of neurofibromatosis type 1: our experience.

A novel mutation in the ZNF462 gene c.3306dup; p.(Gln1103Thrfs*10) is associated to Weiss-Kruszka syndrome. A case report.

Neurological manifestations of neurofibromatosis type 1: our experience.

Functional progression of patients with neurological diseases in a tertiary paediatric intensive care unit: Our experience.

Face recognition impairment in small for gestational age and preterm children.

[Langerhans' cell histiocytosis: various manifestations with the same histopathologic base].

[External ventricular assist devices as circulatory support in patients with dilated cardiomyopathy].

[Comparison of the epidemiological characteristics of neural tube defects classified according to failure of the different points of closure].

[Cutaneous colonization by Malassezia spp. in neonates].

[Balloon valvoplasty for critical aortic valve stenosis in neonates].

[Childhood headache. A diagnostic approach].

Early sodium channel blocker initiation is associated with better outcomes in KCNQ2 disorders.

Palatal Perforation as a Rare Presentation of Severe Congenital Neutropenia Due to an ELANE Mutation.

Median Nerve Entrapment After Intramedullary Nailing of a Pediatric Both-Bone Forearm Fracture: A Rare Case Report.

Relapse of Steroid-Dependent Nephrotic Syndrome Despite Long-Term Ciclosporin Therapy in an 11-Year-Old Child: A Case Report and Review on the Management of Nephrotic Syndrome in Children.

Embryological Basis and Genetic Considerations of Right Lumbar Undescended Caecum with Paracaecal Appendix and Aberrant Vascular Supply.

Inhibition Mechanism of Pancreatic KATP Channels by Centipede Toxin.

Related Experiment Videos

[Neonatal macrocephaly caused by multiple cerebral arteriovenous fistula treated with embolization techniques]

Related Concept Videos

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